Interdependency of Subsurface Carbon ... - ACS Publications

Subscriber access provided by the University of Exeter

Article

Interdependency of Subsurface Carbon Distribution and Graphene-Catalyst Interactions Robert S Weatherup, Hakim Amara, Raoul Blume, Bruno Dlubak, Bernhard C. Bayer, Mamadou Diarra, Mounib Bahri, Andrea Cabrero-Vilatela, Sabina Caneva, Piran R. Kidambi, Marie-Blandine Martin, Cyrile Deranlot, Pierre Seneor, Robert Schlögl, François Ducastelle, Christophe Bichara, and Stephan Hofmann J. Am. Chem. Soc., Just Accepted Manuscript • DOI: 10.1021/ja505454v • Publication Date (Web): 04 Sep 2014 Downloaded from http://pubs.acs.org on September 4, 2014

Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a free service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are accessible to all readers and citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.

Journal of the American Chemical Society is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.

Page 1 of 39

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Journal of the American Chemical Society

Interdependency of Subsurface Carbon Distribution and Graphene-Catalyst Interaction Robert S. Weatherup,1,*, Hakim Amara2, Raoul Blume3, Bruno Dlubak4, Bernhard C. Bayer1, Mamadou Diarra5,6, Mounib Bahri2, Andrea Cabrero-Vilatela1, Sabina Caneva1, Piran R. Kidambi1, Marie-Blandine Martin,4 Cyrile Deranlot 4, Pierre Seneor4, Robert Schloegl7, François Ducastelle2, Christophe Bichara5, and Stephan Hofmann1 1 Dept. of Engineering, University of Cambridge, Cambridge CB3 0FA, UK 2 Laboratoire d’Etude des Microstructures, ONERA-CNRS, BP 72, 92322 Châtillon cedex, France 3 Helmholtz-Zentrum Berlin für Materialien und Energie, D-12489 Berlin, Germany 4 Unité Mixte de Physique CNRS/Thales, 91767 Palaiseau, France, and University of Paris-Sud,

91405 Orsay, France 5 Aix-Marseille Université, CNRS, CINaM UMR 7325, 13288 Marseille, France 6 Physics and Materials Science Research Unit, University of Luxembourg, L-1511, Luxembourg, Luxembourg 7 Fritz Haber Institute, D-14195 Berlin-Dahlem, Germany

ACS Paragon Plus Environment

1


1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 2 of 39

ABSTRACT The dynamics of the graphene-catalyst interaction during chemical vapor deposition are investigated using in situ, time- and depth-resolved X-ray Photoelectron Spectroscopy and complementary grand canonical Monte Carlo simulations coupled to a tight-binding model. We thereby reveal the interdependency of the distribution of carbon close to the catalyst surface and the strength of the graphene-catalyst interaction. The strong interaction of epitaxial graphene with Ni(111) causes a depletion of dissolved carbon close to the catalyst surface, which prevents additional layer formation leading to a self-limiting graphene growth behavior for low exposure pressures (10-6-10-3 mbar). A further hydrocarbon pressure increase (to ~10-1 mbar) leads to weakening of the graphene-Ni(111) interaction accompanied by additional graphene layer formation, mediated by an increased concentration of near-surface dissolved carbon. We show that growth of more weakly adhered, rotated graphene on Ni(111) is linked to an initially higher level of near-surface carbon compared to the case of epitaxial graphene growth. The key implications of these results for graphene growth control and their relevance to carbon nanotube growth are highlighted in the context of existing literature.

KEYWORDS Graphene, chemical vapor deposition (CVD), Nickel (Ni), in situ X-ray photoelectron spectroscopy (XPS), interaction, dissolved carbon, Tight-Binding (TB), Grand Canonical Monte Carlo (GCMC), epitaxy, carbon nanotubes (CNT)


2

Page 3 of 39

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


INTRODUCTION Catalytic techniques for producing graphene and carbon nanotubes (CNTs), particularly those based on chemical vapor deposition (CVD), are widely seen as most promising for achieving the requisite level of control over material structure and quality that is demanded by applications.1,2 Key to growth control is a detailed understanding of the role of the catalyst, which however remains incomplete due the wide parameter space, and more specifically for CNT CVD, the complexity of nanoparticulate catalysts.3 There has been a great deal of recent progress in studying catalyst interactions for growing graphene on planar surfaces.4–8 Such systems have model character in terms of catalytic CVD of all other carbon nanostructures in as much as flat, well-defined catalyst surfaces have been used for decades in surface science as model systems for nanoparticulate catalysts typically used in industrial heterogeneous catalysis.3,9 Recent literature on graphene CVD has focused on the control of nucleation density10–13 and epitaxial6,14,15 or pseudo-epitaxial16,17 relationships that can exist between specific catalyst surfaces and the growing graphene. It is important to note that crucial to CVD growth control is the graphene-catalyst interaction at elevated temperatures during precursor exposure. Under these reaction conditions the physical and chemical state of the catalyst surface is highly dynamic, driven by process conditions and catalyst exposure history,6,7,18,19 and hence the graphene-catalyst interaction can be equally dynamic. Graphene on Ni(111) offers a particularly suitable model system for both theoretical and experimental investigation of the graphenecatalyst interaction during CVD. Given the 1×1 epitaxial match between graphene and Ni(111) and the associated strong interaction,5,14,20 recent literature highlights a surprisingly wide range of process-dependent graphene growth mechanisms on Ni(111),6,21,22 some of which actually result in rotated graphene domains, indicative of a weaker catalyst interaction.6,23 There remain


3


1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 4 of 39

significant disparities in the literature between the growth on thick single crystalline Ni(111) substrates under UHV conditions where monolayer graphene is commonly achieved,6,14,24 and growth on polycrystalline, thin Ni films where the formation of few-layer graphene is typically reported.25–27 Since the growth of a second or further graphene layers occurs at the interface between the catalyst and the existing graphene,28,29 layer control is directly linked to the graphene-catalyst interaction and this further highlights the need for understanding the variations in strength of this interaction. Here we use in situ, time- and depth-resolved X-ray Photoelectron Spectroscopy (XPS)30 and grand canonical Monte Carlo (GCMC) simulations coupled to a tight-binding (TB) model31 to probe and rationalize the process-dependent nature of the graphene-catalyst interaction and how these relate to CVD growth control. We focus on Ni(111) as a model catalyst surface and probe in-operando a wide range of hydrocarbon exposure pressures (10-6-10-1 mbar) as typically used in industrial CVD reactors. Our data reveals an interdependency between the carbon distribution close to the catalyst surface and the strength of the graphene-Ni interaction. Epitaxial graphene formation on Ni(111) leads to a depletion of carbon close to the Ni surface. This prevents the nucleation of further graphene layers and leads to a self-limiting graphene growth behavior at low exposure pressures (10-6-10-3 mbar). A further hydrocarbon pressure increase (to ~10-1 mbar) leads to weakening of the graphene-Ni(111) interaction accompanied by additional graphene layer formation, mediated by an increased concentration of near-surface dissolved carbon. We show that growth of more weakly adhered, rotated graphene on Ni(111) is linked to an initially higher concentration of near-surface carbon. This allows us to consistently explain previous graphene CVD results in the literature. We further discuss the key implications for graphene growth control as well as the relevance of these results to CNT CVD.


4

Page 5 of 39

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


RESULTS Graphene Formation and Stability We experimentally investigate graphene formation and stability on 40nm thick Ni(111) films supported on mono-crystalline sapphire(0001) substrates (see Figure 1 and Methods). Reflection High Energy Electron Diffraction (RHEED) confirms the uniform surface orientation of the catalyst (Figure 1). The samples are exposed to C2H4(10-6-10-1 mbar) at 400°C, following a preannealing step typically performed at 400°C in H2(1 mbar) (see Methods). We emphasize that graphene growth occurs at temperature during the hydrocarbon exposure, and precipitation on cooling is negligible, as expected for the catalyst thickness and growth temperature used.10,27,32 The epitaxial relationship between the sapphire(0001) and Ni(111) averts the dewetting normally expected for such thin catalyst films, even following graphene growth, as confirmed by atomic force microscopy (AFM) measurements which reveal a low rms roughness of only ~0.7nm. We focus here on relatively thin Ni films, which allow the level of dissolved carbon throughout the catalyst to be increased more readily during hydrocarbon exposure than is possible with thicker Ni. To help rationalize our experimental findings, we also perform GCMC simulations of graphene formation and stability on Ni(111) slabs for different temperatures (800-1200 K), and carbon chemical potentials (µC = -7.5 to -5.0 eV/atom) (see Methods). µC is thereby referenced to a fictitious, ideal, monoatomic gas and thus has values of similar order to the cohesive energies of the various carbon phases (e.g., -7.41 eV/atom for a graphene layer in our model). We note that for these simulations, increases in µC correspond qualitatively to experimental increases in hydrocarbon exposure pressure. Additionally, given the melting temperature obtained for pure bulk Ni is ~15% higher than the experimental value,33 the temperatures imposed in our


5


1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60

Page 6 of 39

simulations of 800–1200 K should be rescaled accordingly, and thus correspond to ~400 – 750 °C experimentally. Figures 2A-D show in situ, time-resolved XP C1s core level spectra measured on the Ni(111) surfaces during C2H4 (10-6 mbar) exposure at ~400°C (see Methods). In this context, timeresolved refers to scan times of tens of seconds, whilst the observed growth evolution proceeds over hours. We assign four principal components, which have been systematically refined on the basis of extensive CNT19,34,35 and graphene7,10,13,27 growth experiments and previous literature:36– 40

CA (283.2 eV) relates to carbon bonded at Ni surface sites, CDis (283.8 eV) to interstitial

carbon dissolved in the Ni lattice,10 CGr (284.4 eV) to relatively weakly interacting graphene layers (including rotated graphene, additional graphene layers, or graphene decoupled from the Ni surface,6,23) and CB (284.8 eV) to strongly interacting epitaxial graphene on Ni(111).6 We thus define the strength of the graphene-catalyst interaction on the basis of this shift in binding energy between CGr and CB. On exposure of the clean Ni surface (Figure 2A) to C2H4(10-6 mbar), we observe the same C1s peak evolution as we previously reported for the growth on thick (~1 mm) Ni(111) single crystals under similar growth conditions.6 The CA peak emerges ~1min after hydrocarbon introduction, gradually growing in intensity over ~10mins (Figure 2B), and for these conditions is assigned to a structural surface carbide, Ni2C.6 A small contribution from a species at lower binding energy (~282.9 eV) is also observed, which may reflect carbon in a different bonding environment at the Ni surface. As the C2H4 exposure continues, the CB peak emerges (Figure 2C), and grows in intensity at the expense of the CA peak and eventually becomes dominant (Figure 2D). A weak CGr peak is also present, but remains a minority component throughout. The observed growth mode is thus the formation of epitaxial monolayer graphene via the


6

Page 7 of 39

1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60


transformation of Ni2C.6 The CDis peak also remains rather weak, as expected in light of the low solubility of carbon in Ni at this temperature.32 The XP spectrum changes little during further exposure, indicating the stability of this epitaxial graphene monolayer under these conditions. Figures 2E-G show the effect on the as-formed graphene sample of stepwise increases in the C2H4 exposure pressure from 10-6 mbar to 10-1 mbar. We note that increasing exposure pressures correspond to an increased carbon supply to the catalyst surface fed through defects in the asformed graphene,41–44 which may include atom vacancies, substitutional catalyst atoms,6 StoneWales like defects,45 and line46/grain-boundary defects. Up to 10-3 mbar, there is a slight decrease in total XP signal related to increasing scattering of the photoelectrons by gas molecules, however the relative intensities of the spectral components remain constant (Figure 2E). We thus confirm no significant change in the epitaxial graphene despite an increase in the feedstock pressure by three orders of magnitude, demonstrating that epitaxial monolayer graphene is stable across a broad pressure window. On increasing the exposure pressure further to 10-1 mbar, the XP signal decreases significantly as the scattering of the photoelectrons becomes more severe.30 Most importantly however, a significant shift in the majority peak from CB towards CGr occurs as the exposure proceeds (Figures 2 F,G). A notable increase in the intensity of the CDis peak is also simultaneously observed, reflecting an increase in the quantity of interstitial carbon dissolved in the Ni lattice close to the surface.10 On removal of the C2H4 (10-1 mbar) and subsequent pumping to

Interdependency of Subsurface Carbon ... - ACS Publications

Recommend Documents